Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem development
Laura Powell(University of Maryland, Baltimore), John A. Sayer(Newcastle University), Simon A. Ramsbottom(Newcastle University), Laura A. Devlin(Newcastle University), Gavin J. Clowry(Newcastle University), C. G. Miles(Newcastle University), Miguel Barroso‐Gil(Clinical Research Institute), Elisa Molinari(Newcastle University)
Cited by 7
Related Papers
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
|Nature Genetics|2006|579
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
|Nature Genetics|2005|404
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
|Cell|2012|392
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse
|Human Molecular Genetics|2006|381
Germline selection shapes human mitochondrial DNA diversity
|Science|2019|253